Hetero walk-in qc,qa,Engineering,Production,Packing
- Company Overview
- Job Role & Responsibilities
- QUALITY CONTROL – Formulation
- PRODUCTION – Formulation Manufacturing
- PACKING – Pharmaceutical Packaging Operations
- QUALITY ASSURANCE – IPQA & QMS
- ENGINEERING – Process Maintenance (Electrical)
- Eligibility / Qualifications
- Location & Walk-in Details
- Documents to Carry
- Why This Opportunity Matters for Pharma Professionals
- Career Growth & Salary Insights
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Who can attend this walk-in drive?
- 2. Are freshers eligible?
- 3. Is prior HPLC or production machine experience mandatory?
- 4. What documents are compulsory?
- 5. Is this opportunity suitable for regulatory market experience?
- Walk-in Drive Summary
BPharm MSc ITI Diploma Vacancies at Hetero Unit III
BPharm, MSc, ITI, Diploma candidates – multiple vacancies at Hetero Unit III Jeedimetla. 1–6 yrs experience. Walk-in on 28 Feb 2026.
Hetero is conducting a major walk-in drive for multiple departments at its Unit III facility in Jeedimetla, Hyderabad. This hiring initiative targets skilled professionals from pharmaceutical manufacturing, quality control, quality assurance, engineering, and packing operations. Candidates with 1 to 6 years of experience in regulated pharma environments are encouraged to attend. If you are looking for growth in pharmaceutical manufacturing, GMP compliance, quality systems, or production operations, this opportunity offers strong career progression within a reputed global pharmaceutical organization.
Company Overview
Hetero is one of India’s leading pharmaceutical companies with a strong global presence in active pharmaceutical ingredients (API) and finished dosage formulations. The organization supplies medicines across regulated and semi-regulated markets and plays a significant role in improving access to affordable healthcare worldwide.
The company operates advanced manufacturing facilities that follow stringent regulatory standards such as cGMP, USFDA, MHRA, and WHO-GMP guidelines. Unit III at Jeedimetla is a key formulation manufacturing site contributing to solid oral dosage production and quality-driven pharmaceutical operations.
Working at Hetero provides exposure to:
- Regulatory-compliant pharmaceutical manufacturing
- Advanced analytical laboratories (HPLC, GC, Dissolution, Stability testing)
- Quality Management Systems (QMS) and IPQA operations
- Engineering and process maintenance systems
- Global pharmaceutical supply chain standards
This walk-in drive reflects Hetero’s expansion plans and continued investment in pharmaceutical manufacturing excellence.
Job Role & Responsibilities
QUALITY CONTROL – Formulation
Designations: Jr. Officer, Officer, Jr. Executive, Executive
Experience Required: 1–6 Years
Qualification: B Pharm, M Pharm, MSc
Key Responsibilities:
- Handling analytical instruments such as HPLC and GC
- Performing dissolution testing and wet analysis
- Conducting stability studies (IP/FP)
- Raw material (RM) testing and documentation
- Working within LIMS systems
- Ensuring GLP compliance
- Supporting microbiology testing where applicable
- Maintaining data integrity in laboratory operations
Candidates must have strong exposure to pharmaceutical quality control processes in regulated environments.
PRODUCTION – Formulation Manufacturing
Designations: Jr Operator, Operator, Jr Officer, Officer, Jr Executive, Executive
Experience Required: 1–6 Years
Qualification: ITI, Diploma, BSc, B Pharm
Key Responsibilities:
- Operating granulation equipment
- Compression machine handling
- Coating operations including Wurster coating
- Capsule filling processes
- Roll compactor operation
- Batch manufacturing documentation
- Ensuring GMP compliance on shop floor
Experience in solid oral dosage manufacturing is preferred. Candidates must understand production SOPs, deviation handling, and in-process checks.
PACKING – Pharmaceutical Packaging Operations
Designations: Jr Operator, Operator, Jr Officer, Officer, Jr Executive, Executive
Experience Required: 1–6 Years
Qualification: ITI, Diploma, BSc, B Pharm
Key Responsibilities:
- Blister packing operations
- Bottle packing lines
- Liquid filling support
- Track & Trace system handling
- Packaging documentation and reconciliation
- Ensuring compliance with packaging validation protocols
Experience in automated packing lines within pharma formulation units is highly desirable.
QUALITY ASSURANCE – IPQA & QMS
Designations: Jr Officer, Officer, Jr Executive, Executive
Experience Required: 1–6 Years
Qualification: B Pharm, M Pharm, MSc
Key Responsibilities:
- In-Process Quality Assurance (IPQA)
- Handling Quality Management Systems (QMS)
- Deviation management and CAPA tracking
- Batch record review
- Line clearance and GMP audits
- Documentation review for regulatory inspections
Candidates should have exposure to pharmaceutical compliance standards and regulatory inspection readiness.
ENGINEERING – Process Maintenance (Electrical)
Designations: Technician, Jr Engineer, Engineer, Jr Executive
Experience Required: 1–6 Years
Qualification: Diploma, B Tech
Key Responsibilities:
- Electrical process maintenance
- Preventive and breakdown maintenance
- Calibration coordination
- Utility systems monitoring
- Supporting production equipment uptime
Strong technical knowledge in pharmaceutical plant maintenance systems is required.
Eligibility / Qualifications
Candidates must possess relevant educational qualifications based on department requirements.
Eligible Courses Include:
B Pharm, M Pharm, MSc (Chemistry, Analytical Chemistry, Microbiology, Biotechnology), BSc (Chemistry, Life Sciences), Diploma in Pharmacy, Diploma in Mechanical Engineering, Diploma in Electrical Engineering, ITI (Fitter, Electrician, Mechanical), B Tech (Electrical, Mechanical)
Additional Requirements:
- 1 to 6 years of relevant pharmaceutical industry experience
- Experience in GMP-compliant manufacturing units
- Exposure to regulatory audits preferred
- Strong documentation and data integrity practices
Freshers are not specified for this drive. Relevant hands-on experience is mandatory.
Location & Walk-in Details
Work Location: Unit III, Jeedimetla, Hyderabad
Interview Date: 28th February 2026 (Saturday)
Timings: 9:30 AM to 3:00 PM
Venue Address:
Hetero Labs Limited
Unit III
22-110, IDA, Jeedimetla
Hyderabad
Documents to Carry
Candidates must bring:
- Updated Resume
- Educational Certificates
- Last 3 months’ salary slips
- Appointment letters from previous employers
- Current CTC details
- Government ID proof (Aadhar or PAN)
Incomplete documentation may delay the interview process.
For further information, candidates may contact:
Email: chandrasekhar.r@hetero.com
Why This Opportunity Matters for Pharma Professionals
The pharmaceutical industry in Hyderabad continues to expand rapidly. Jeedimetla is a major pharma manufacturing hub offering stable employment and long-term career growth. Roles in Quality Control, Quality Assurance, Production, and Engineering are considered high-demand pharmaceutical careers due to regulatory complexity and global supply chain importance.
Professionals with experience in HPLC analysis, GMP manufacturing, pharmaceutical production operations, IPQA compliance, and process maintenance are positioned strongly for salary growth and leadership roles.
Hetero’s continued hiring signals operational expansion and regulatory market penetration. Working in such an environment builds technical credibility and strengthens your profile for future opportunities in USFDA-approved manufacturing units.
Career Growth & Salary Insights
While specific salary details are not disclosed, industry benchmarks for professionals with 1–6 years of pharmaceutical experience in Hyderabad typically range based on role and expertise. Candidates with regulatory exposure, audit experience, and specialized technical skills (HPLC, GC, QMS, IPQA, Electrical Maintenance) generally command higher compensation packages.
Performance-driven promotions, regulatory exposure, and cross-functional experience significantly enhance long-term career prospects in pharma manufacturing.
Application Process
This is a direct walk-in interview process. No prior online application is mandatory.
Steps to Apply:
- Prepare updated resume.
- Arrange all required documents.
- Visit the venue on 28th February 2026 between 9:30 AM and 3:00 PM.
- Attend technical and HR interview rounds.
Candidates are advised to arrive early to avoid crowd delays.
Frequently Asked Questions (FAQs)
1. Who can attend this walk-in drive?
Candidates with 1–6 years of experience in pharmaceutical manufacturing, quality control, quality assurance, packing, or engineering roles can attend.
2. Are freshers eligible?
This drive specifically mentions 1–6 years of experience. Freshers are not indicated as eligible.
3. Is prior HPLC or production machine experience mandatory?
Yes. Relevant hands-on exposure in the mentioned functional areas is expected.
4. What documents are compulsory?
Resume, educational certificates, last three salary slips, appointment letters, CTC details, and valid ID proof.
5. Is this opportunity suitable for regulatory market experience?
Yes. Exposure to GMP, GLP, IPQA, and QMS makes it highly valuable for professionals targeting regulated market pharmaceutical careers.
Walk-in Drive Summary
| Company | Hetero Labs Limited |
|---|---|
| Vacancies | Quality Control – Jr Officer/Officer/Jr Executive/Executive; Production – Jr Operator/Operator/Jr Officer/Officer/Jr Executive/Executive; Packing – Jr Operator/Operator/Jr Officer/Officer/Jr Executive/Executive; Quality Assurance – Jr Officer/Officer/Jr Executive/Executive; Engineering – Technician/Jr Engineer/Engineer/Jr Executive |
| Required Education | B Pharm, M Pharm, MSc, BSc, ITI, Diploma, B Tech |
| Experience | 1–6 Years |
